LivingGLP1
Study S000158

A Study to Investigate the Efficacy and Safety of Orforglipron Once Daily in Participants With Peripheral Artery Disease: A Randomized, Double-Blind, Placebo Controlled Trial

Registration

Registration
NCT07223593
Acronym
ATTAIN-PAD
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
RECRUITING
Enrollment
1205
Start
2025-10-31
Primary completion
2028-06
Lead sponsor
Eli Lilly and Company
Conditions
Peripheral Arterial Disease
Interventions
DRUG:Orforglipron; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2025-523283-21-00; OTHER:J2A-MC-GZPR; NIH:2025

Registered primary outcomes

  • Percent Change from Baseline in Maximum Walking Distance [Baseline, Week 52]

Linked records (0)

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